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Results 1 - 10 of 89 for Autosomal anomaly
  1. Fryns syndrome 
    ... KL, Saal HM, Stern HJ. Fryns syndrome: an autosomal recessive disorder associated with craniofacial anomalies, diaphragmatic hernia, and distal digital hypoplasia. Pediatrics. 1990 ...
    https://medlineplus.gov/genetics/condition/fryns-syndrome - Genetics
  2. Spondylocarpotarsal synostosis syndrome 
    ... Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies. Hum Mutat. 2017 May;38(5):540-547. ...
    https://medlineplus.gov/.../spondylocarpotarsal-synostosis-syndrome - Genetics
  3. FLNB gene 
    ... Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies. Hum Mutat. 2017 May;38(5):540-547. ...
    https://medlineplus.gov/genetics/gene/flnb - Genetics
  4. Learning about Velocardiofacial Syndrome From the National Institutes of Health (National Human Genome Research Institute)  
    National Human Genome Research Institute ... From the National Institutes of Health ... Parathyroid Disorders/Genetics ... Parathyroid Disorders ... Cleft Lip and Palate/ ...
    https://www.genome.gov/Genetic-Disorders/Velocardiofacial-Syndrome - National Institutes of Health
  5. 22q11.2 deletion syndrome 
    ... members may be affected as well. 22q11.2DS Autosomal dominant Opitz G/BBB syndrome CATCH22 Cayler cardiofacial syndrome Conotruncal anomaly face syndrome (CTAF) Deletion 22q11.2 syndrome DiGeorge ...
    https://medlineplus.gov/genetics/condition/22q112-deletion-syndrome - Genetics
  6. BOR Syndrome From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Genetic and Rare Diseases Information Center ... From the National Institutes of Health ... Birth Defects/Specifics ... Birth Defects ... Find symptoms and other information ...
    https://rarediseases.info.nih.gov/diseases/10147/bor-syndrome - National Institutes of Health
  7. ADNP syndrome 
    ... Helsmoortel-van der Aa syndrome HVDAS Mental retardation, autosomal dominant 28 MRD28 Genetic Testing Registry: ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder ADNP syndrome National ...
    https://medlineplus.gov/genetics/condition/adnp-syndrome - Genetics
  8. Isolated Duane retraction syndrome 
    ... caused by CHN1 gene variants, it has an autosomal dominant inheritance pattern. Co-contractive retraction syndrome Duane anomaly, isolated Duane retraction syndrome Duane syndrome Duane's ...
    https://medlineplus.gov/.../isolated-duane-retraction-syndrome - Genetics
  9. 22q11.2 Deletion Syndrome (DiGeorge Syndrome) (For Parents) (Nemours Foundation)  
    ... 22q, 22q11.2DS, DiGeorge syndrome, DiGeorge, Shprintzen Syndrome, autosomal dominant OpitzG, Cayler Cardiofacial Syndrome, cardiofacial, Conotruncal Anomaly Face Syndrome, Velocardiofacial Syndrome,
    https://kidshealth.org/en/parents/22q11-deletion.html - External Health Links
  10. Adams-Oliver syndrome 
    ... M. DOCK6 mutations are responsible for a distinct autosomal-recessive variant of Adams-Oliver syndrome associated with brain and eye anomalies. Hum Mutat. 2015 Jun;36(6):593-8. ...
    https://medlineplus.gov/genetics/condition/adams-oliver-syndrome - Genetics
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